polyclonal goat anti mouse il 33 antibody  (R&D Systems)

Journal: Blood Advances

Article Title: The alarmin interleukin-33 modulates platelet proteome, function, and biogenesis

doi: 10.1182/bloodadvances.2025018363

Figure Lengend Snippet: IL-33 is not expressed by circulating platelets or MKs. (A-B) Representative immunofluorescence images showing nonspecific IL-33 staining in bone marrow (BM)–derived MKs enriched on BSA gradient (A) and platelet-rich plasma (PRP) (B) from WT and IL-33KO mice. (C) Flow-cytometric detection of IL-33 nonspecific signal in blood platelets from WT and IL-33KO mice (PRP), using an isotype control as a negative reference. (D) Western blot analysis of IL-33 expression in platelets and MK-enriched BM cells, with total lung lysates from WT and IL-33 KO mice used as positive and negative controls, respectively. Following quantification, an equal amount of protein (20 μg) was loaded in each lane. (E) IL-33 promoter activity in total BM cells, blood platelets, and BM MK from IL-33–Citrine reporter mice assessed by flow cytometry. (F) Identification of Citrine + cells as stromal cells (CD41 − CD45 − ) in Citrine reporter mice (Citrine +/+ ) by flow cytometry. Panels A-D used a polyclonal goat anti-mouse IL-33 antibody. FL, full length; IF, immunofluorescence; KO, knockout; mIL, mouse interleukin; SSC-A, side scatter.

Article Snippet: However, IL-33 mRNA and protein have not been detected in previous platelet transcriptomic or proteomic studies., To resolve these discrepancies, we performed analyses with a polyclonal goat anti-mouse IL-33 antibody (R&D Systems, catalog no. AF3626) that has been validated for immunofluorescence, flow cytometry, and western blot analyses in previous studies , including several studies by our team., , , IL-33 is a nuclear cytokine and the Ab AF3626 stains the nucleus of IL-33 producing cells in WT mice but not in IL-33KO mice.

Techniques: Immunofluorescence, Staining, Derivative Assay, Clinical Proteomics, Control, Western Blot, Expressing, Activity Assay, Flow Cytometry, Knock-Out

Journal: Blood Advances

Article Title: The alarmin interleukin-33 modulates platelet proteome, function, and biogenesis

doi: 10.1182/bloodadvances.2025018363

Figure Lengend Snippet: IL-33 deficiency alters the platelet proteome. (A) Proteomic profiling of sorted platelets from WT and IL-33KO mice. (B) Volcano plot comparing IL-33KO and WT platelet proteomes. The x-axis shows log fold change (IL-33KO/WT), and the y-axis shows −log( P -value). Proteins upregulated in IL-33KO platelets are highlighted in blue; downregulated proteins in gray. (C) Number of proteins detected and significantly altered ( P < .03, fold change > 0.2). (D,F) Gene Ontology (GO) analysis of enriched biological processes among upregulated (D) and downregulated (F) proteins ( https://geneontology.org ). (E,G) Heat maps of the top 20 most abundant upregulated (E) and downregulated (G) proteins. Data were obtained from n = 5 mice per group. KO, knockout. Figure created with biorender.com . Blanchard L. (2026) https://BioRender.com/b78qj95 .

Article Snippet: However, IL-33 mRNA and protein have not been detected in previous platelet transcriptomic or proteomic studies., To resolve these discrepancies, we performed analyses with a polyclonal goat anti-mouse IL-33 antibody (R&D Systems, catalog no. AF3626) that has been validated for immunofluorescence, flow cytometry, and western blot analyses in previous studies , including several studies by our team., , , IL-33 is a nuclear cytokine and the Ab AF3626 stains the nucleus of IL-33 producing cells in WT mice but not in IL-33KO mice.

Techniques: Knock-Out

Journal: Blood Advances

Article Title: The alarmin interleukin-33 modulates platelet proteome, function, and biogenesis

doi: 10.1182/bloodadvances.2025018363

Figure Lengend Snippet: IL-33 deficiency impairs platelets adhesion to ECM components. (A) Schematic and (B) analysis of platelet adhesion assays to soluble fibrinogen, with or without ADP (1μM), assessed by flow cytometry. PRP from WT and IL-33 KO mice was analyzed, and results are expressed as a ratio relative to the WT mean. Data were obtained from n = 11 mice per group across 3 independent experiments. (C) Schematic of platelet spreading assays on fixed substrates, analyzed by immunofluorescence in WT and IL-33 KO platelets. Representative images and quantitative analyses of adherent and spreading PRP from WT or IL-33 KO mice on (D) fibrinogen, (E) podoplanin, and (F) laminin at 5 and 15 minutes following ADP (1μM) stimulation. Platelets were stained with CD41-APC. Data were obtained from n = 11 mice per group across 3 independent experiments, except for the laminin spreading assay, which was performed on n = 5 mice in a single experiment. (G-H) Platelet spreading assays without ADP stimulation on fibrinogen (G) and podoplanin (H) at 5 and 15 minutes (n = 7 mice per group per experiment). Statistical analyses were performed using t tests (D-F) and 2-way analysis of variance (ANOVA) with Sidak multiple comparisons test (B). Scale bar, 20 μm. Statistical analysis was conducted using t tests; # P < .05; ## P < .01; ### P < .001; #### P < .0001. IF, immunofluorescence. Figure created with biorender.com . Blanchard L. (2026) https://BioRender.com/z523pur .

Article Snippet: However, IL-33 mRNA and protein have not been detected in previous platelet transcriptomic or proteomic studies., To resolve these discrepancies, we performed analyses with a polyclonal goat anti-mouse IL-33 antibody (R&D Systems, catalog no. AF3626) that has been validated for immunofluorescence, flow cytometry, and western blot analyses in previous studies , including several studies by our team., , , IL-33 is a nuclear cytokine and the Ab AF3626 stains the nucleus of IL-33 producing cells in WT mice but not in IL-33KO mice.

Techniques: Flow Cytometry, Immunofluorescence, Staining

Journal: Blood Advances

Article Title: The alarmin interleukin-33 modulates platelet proteome, function, and biogenesis

doi: 10.1182/bloodadvances.2025018363

Figure Lengend Snippet: IL-33 deficiency reduces thrombus formation under high shear stress. (A) Schematic representation of the thrombus formation assay on collagen during arterial flow of whole blood from WT or IL-33 KO mice. (B) Representative images and quantitative analysis of thrombus volume, expressed as a percentage relative to the WT mean, formed on collagen under physiological arterial shear rate (1500 s ˗1 ) using whole blood from WT or IL-33 KO mice. (C) Representative images and quantitative analysis of thrombus volume, expressed as a percentage relative to the WT mean, formed on collagen under pathological arterial shear rate (3000 s ˗1 ) using whole blood from WT or IL-33 KO mice. Data are representative of 3 independent experiments (n = 4-5 mice/group). Statistical analysis was performed using 2-way ANOVA with Sidak multiple comparisons test, # P < .05. Investigators were blinded to genotype during the thrombus formation assay. Figure created with biorender.com . Blanchard L. (2026) https://BioRender.com/tt7i113 .

Article Snippet: However, IL-33 mRNA and protein have not been detected in previous platelet transcriptomic or proteomic studies., To resolve these discrepancies, we performed analyses with a polyclonal goat anti-mouse IL-33 antibody (R&D Systems, catalog no. AF3626) that has been validated for immunofluorescence, flow cytometry, and western blot analyses in previous studies , including several studies by our team., , , IL-33 is a nuclear cytokine and the Ab AF3626 stains the nucleus of IL-33 producing cells in WT mice but not in IL-33KO mice.

Techniques: Shear, Tube Formation Assay

Journal: Blood Advances

Article Title: The alarmin interleukin-33 modulates platelet proteome, function, and biogenesis

doi: 10.1182/bloodadvances.2025018363

Figure Lengend Snippet: IL-33 treatment in vivo modifies platelet morphology and activation, expands the MK-biased LT-HSC pool, and enhances platelet release within lung capillaries. (A) Schematic overview of the IL-33 treatment protocol: WT mice received 3 intranasal doses of recombinant human IL-33 or PBS. (B) Flow cytometry analysis of platelet morphology in WT mice following IL-33 or PBS treatment. (C) Quantification of platelet counts by flow cytometry in IL-33- or PBS-treated WT mice. Data are from n = 14 mice per group, collected across 3 independent experiments. (D) Flow cytometry assessment of platelet degranulation, measuring alpha granule (P-selectin) and dense granule (CD63) expression after IL-33 or PBS administration. (E) Plasma levels of sCD40L, measured by ELISA in IL-33–treated or PBS-treated WT mice. (D-E) Data are from n = 8 to 9 mice per group, collected across 2 independent experiments. (F) Quantification of BM LT-HSC, separated into CD41 ˗ (canonical) and CD41 + (MK-biased) populations, shown as a percentage of LSK cells. Data are obtained from n = 22 mice per group, collected across 5 independent experiments. (G) Lung intravital microscopy was performed in PF4-mTmG mice treated with IL-33 or PBS, 24 hours after the first (IL-33 1×) or third (IL-33 3×) administration to assess MKs/proplatelets generating platelets. (H) Representative time-lapse intravital lung microscopy images showing PF4 + small proplatelets and large proplatelet/MK structures releasing platelets within pulmonary capillaries. Scale bar, 50 μm. (I-J) Quantification of proplatelet structures producing platelets per hour per ROI in the lung, categorized as small (<200 platelet volume equivalent), medium (200-1000 platelets), and large (>1000 platelets). (K) Total platelet release per hour across the entire lung. Statistical analysis was performed using t test; # P < .05, ## P < .01. A total of n = 5 to 21 videos were analyzed, collected from 3 to 11 mice per group across 5 independent experiments. ns, not significant. Figure created with biorender.com . Blanchard L. (2026) https://BioRender.com/qdgtyov .

Article Snippet: However, IL-33 mRNA and protein have not been detected in previous platelet transcriptomic or proteomic studies., To resolve these discrepancies, we performed analyses with a polyclonal goat anti-mouse IL-33 antibody (R&D Systems, catalog no. AF3626) that has been validated for immunofluorescence, flow cytometry, and western blot analyses in previous studies , including several studies by our team., , , IL-33 is a nuclear cytokine and the Ab AF3626 stains the nucleus of IL-33 producing cells in WT mice but not in IL-33KO mice.

Techniques: In Vivo, Activation Assay, Recombinant, Flow Cytometry, Expressing, Clinical Proteomics, Enzyme-linked Immunosorbent Assay, Intravital Microscopy, Microscopy

Journal: Blood Advances

Article Title: The alarmin interleukin-33 modulates platelet proteome, function, and biogenesis

doi: 10.1182/bloodadvances.2025018363

Figure Lengend Snippet: IL-33 in vivo treatment alters platelet proteome, modulating inflammatory and coagulation-related pathways. (A) Proteomic profiling of sorted platelets from WT mice treated with PBS or recombinant (rIL-33). (B) Volcano plot comparing human rIL-33 and PBS-treated mice platelet proteomes. The x-axis shows log fold change (IL-33KO/WT), and the y-axis shows ˗log( P -value). Proteins upregulated in IL-33 treated mice platelets are highlighted in orange; downregulated proteins in gray. (C) Number of proteins detected and significantly altered ( P < .03, fold change > 0.2). (D,F) Gene Ontology (GO) analysis of enriched biological processes among upregulated (D) and downregulated (F) proteins ( https://geneontology.org ). (E,G) Heat maps of the top 20 most abundant upregulated (E) and downregulated (G) proteins. Data represent n = 10 mice per group, collected from 2 independent experiments. Figure created with biorender.com . Blanchard L. (2026) https://BioRender.com/og48c3y .

Article Snippet: However, IL-33 mRNA and protein have not been detected in previous platelet transcriptomic or proteomic studies., To resolve these discrepancies, we performed analyses with a polyclonal goat anti-mouse IL-33 antibody (R&D Systems, catalog no. AF3626) that has been validated for immunofluorescence, flow cytometry, and western blot analyses in previous studies , including several studies by our team., , , IL-33 is a nuclear cytokine and the Ab AF3626 stains the nucleus of IL-33 producing cells in WT mice but not in IL-33KO mice.

Techniques: In Vivo, Coagulation, Recombinant

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Freshly isolated eWAT-Treg cells from 12wk-old male Foxp3.Thy1.1 mice were cultured with or without Irisin/HSP90α for 3 days, followed by flow-cytometric analysis. Left: experimental scheme; right: summary data for total Treg numbers and fraction of ST2 + Treg cells. n=3. (B) Summary data for numbers of IL-33 + mSCs from the mice in Figure 2A (n=3, 3, 6, 7). One-way ANOVA was used for calculating p values (* p=0.0127). (C) ELISA measurements of IL-33 concentration in eWAT lysates from mice in Figure 1E (n=3, 3, 6, 6). One-way ANOVA was used for calculating p values (** p=0.0019, **** p<0.0001, and **** p<0.0001). (D) ELISA measurements of IL-33 concentration in plasma from mice in Figure 1E (n=6, 9). Unpaired two-sided T-test was used for calculating p values (* p=0.0342). (E) Freshly isolated IL-33 (EGFP) + or IL-33 (EGFP) − mSCs from 12-wk-old male Il33.Egfp mice were cultured with PBS or the indicated concentrations of Irisin/HSP90α for 3 days, followed by flow-cytometric analysis. Left: experimental scheme; right: summary data for numbers and MFI of IL-33 (EGFP) + mSCs. n=4. One-way ANOVA was used for calculating p values (** p=0.0019, *** p=0.0006, **** p<0.0001). (F) Freshly isolated IL-33 (EGFP) − mSCs from 12 wk-old male Il33.Egfp mice were cultured with PBS or 10 nM Irisin/HSP90α for 3 days, and the conditioned medium treated with either control IgG or anti-IL-33 antibody (2 μg/ml) was subsequently used for culturing freshly isolated eWAT Treg cells for another 3 days followed by flow-cytometric analysis. Top: experimental scheme; bottom: summary data for fractions (left) and numbers (right) of ST2 + Treg cells (n=2, 3, 5). One-way ANOVA was used for calculating p values (left: ****p<0.0001, ** p=0.00156, and **** p<0.0001; right: **** p<0.0001, * p=0.0122, and **** p<0.0001). (G) Volcano plot showing transcripts differentially expressed (FC>2, p<0.05) by IL-33 (EGFP) − mSCs cultured with PBS or 10 nM Irisin/HSP90α for 3 days (left). Transcripts from an adipogenesis up-signature are highlighted in magenta (right). Triplicate samples. wk, weeks; PBS, Phosphate-buffered saline; mSCs, mesenchymal stromal cells; other abbreviations as per Figure 1 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Unless specifically mentioned, experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Expressing, Isolation, Cell Culture, Enzyme-linked Immunosorbent Assay, Concentration Assay, Clinical Proteomics, Control, Saline

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Flow-cytometric analysis of IL-33 + mSCs from 16 wk-old male Fndc5 +/+ (n=6) or Fndc5 −/− (n=5) littermates. Left: Representative gating strategy for analyzing IL-33 + mSCs; right: summary data for numbers of total as well as fractions of IL-33 + mSCs. Unpaired two-sided T-test was used for calculating p values (**** p<0.0001). (B) Flow-cytometric analysis of eWAT-Treg cells from 16 wk-old male Fndc5 +/+ (n=6) or Fndc5 −/− (n=5) littermates. Left: Representative gating strategy for analyzing total (black) and ST2 + (red) eWAT-Treg cells; right: summary data for numbers of CD4 + cells, as well as fractions of total and ST2 + Treg cells. Unpaired two-sided T-test was used for calculating p values (** p=0.0031, and ** p=0.0083). (C-D) 8 wk-old male Fndc5 +/+ or Fndc5 −/− littermates were i.p. injected with PBS or IL-33 (40 ng/g body weight) twice a week and were sacrificed 3 days after the last injection. n=6-9. (C) Experimental scheme; (D) Upper: representative gating strategy for analyzing total (black) and ST2 + (red) eWAT-Treg cells; Lower: summary data for numbers of CD4 + cells, as well as fractions of total and ST2 + Treg cells. n=9, 9, 6, 8. One-way ANOVA was used for calculating p values (left: ** p=0.0027, and ** p=0.0037, middle: **** p<0.0001, and **** p<0.0001, right: **** p<0.0001, * p=0.0102, and **** p<0.0001). Abbreviations as per Figure 1 , 2 & 3 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Unless specifically mentioned, experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Injection

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Schematic of HFD feeding experiment with male FNDC5 null mice. 4 wk-old Fndc5 +/+ or Fndc5 −/− littermates were injected with AAV-irisin or -GFP via tail vein and then started HFD feeding after 5 weeks. Experiments were performed at the indicated time points. (B) Body composition analysis by MRI after 17 weeks of HFD feeding (n=6, 5, 6, 5). Two-way ANOVA was used for calculating p values (* p=0.0200, *** p=0.0005, and * p=0.0357). (C) GTTs (upper) and ITTs (lower) analysis of the indicated mice fed a HFD for 16 weeks (n=4, 5, 7, 8). Two-way ANOVA was used for calculating p values (GTT: *** p=0.0001, **** p<0.0001, and **** p<0.0001; ITT: * p=0.0163, **** p<0.0001, and **** p<0.0001). (D) ELISA measurements of IL-33 concentration in eWAT lysates (left, n=7, 6, 7, 4) and in plasma (right, n=4, 4, 4, 4) from indicated mice fed a HFD for 18 weeks. Brown-Forsythe and Welch ANOVA was used for calculating p values (left: ** p=0.0072, * p=0.0147, and *** p=0.0004; right: * p=0.0498, * p=0.0399, and ** p=0.0097). Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Experiments were repeated three times with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Injection, Enzyme-linked Immunosorbent Assay, Concentration Assay, Clinical Proteomics

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Schematic of HFD feeding experiment with long-term IL-33trap treatment. IL-33trap treatments (twice a week, 100 μg/mice/time) started in the same week of diet switch, and the flow analysis was performed with male mice fed a HFD for 18 weeks. (B-D) Flow-cytometric analysis of the number of total CD4 + T cells (B left) , the fractions of total ( B middle) and ST2 + (B right) Treg cells, the number of total mSCs (D left) and the fraction of IL-33 + mSCs (D right) . n=6, 6, 6, 6. One-way ANOVA was used for calculating p values ( B : left: **** p<0.0001, and **** p<0.0001; middle: **** p<0.0001, **** p<0.0001, and **** p<0.0001; right: **** p<0.0001, **** p<0.0001, and **** p<0.0001; C : ** p=0.0026, and **** p<0.0001; D : **** p<0.0001, and **** p<0.0001). (E) Body composition analysis of the indicated mice by MRI after 18 weeks of HFD feeding (n=6, 6, 6, 6). One-way ANOVA was used for calculating p values (* p=0.0108, and * p=0.0202). (F) GTTs (left) and ITTs (right) analysis of the indicated mice fed a HFD for 17 weeks (n=6, 6, 6, 6). Two-way ANOVA was used for calculating p values (GTT: **** p<0.0001, and **** p<0.0001; ITT: **** p<0.0001, and **** p<0.0001). (G) Energy expenditure measured in CLAMS cages over one week. n=4, 4, 4, 4. The last 4 days of measurement were shown on the left and the averaged values in the light and dark periods were summarized on the right. Two-way ANOVA was used for calculating p values (p values between AAV-irisin PBS and AAV-irisin IL-33trap: left: ** p<0.0046, * p<0.0162, ** p<0.0036, and ** p<0.0011; right: ** p=0.0045, and * p=0.0285). (H) RT-qPCR measuring mRNAs associated with thermogenesis and adipogenesis in iWAT of the mice received AAV-irisin or -GFP, treated with IL-33trap and fed a HFD for 18 weeks (n= 3, 3, 3, 3). Two-way ANOVA was used for calculating p values (p values between AAV-GFP PBS and AAV-irisin PBS, as well as AAV-irisin PBS and AAV-irisin IL-33trap: Fabp4 : * p=0.0222, and * p=0.0488; Ucp1: **** p<0.0001, and **** p<0.0001; Alpl: ** p=0.0064, and * p=0.0127; Dio2: **** p<0.0001, and **** p<0.0001; Elovl3: **** p<0.0001, and **** p<0.0001; Cox8b: ** p=0.0027, and ** p=0.0063; Cidea: *** p=0.0003, and *** p=0.0008). Abbreviations as per Figure 1 , 2 & 3 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Unless specifically mentioned, experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Inhibition, Quantitative RT-PCR

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Schematic of HFD feeding experiment with male ST2 Treg null mice ( Il1rl1 Δtreg ) and their littermates ( Il1rl1 wt ). Mice were received AAV-irisin or -GFP at 4 wk-old and then fed a HFD for 17 weeks. GTTs and ITTs were performed with mice fed a HFD for 12 weeks. Flow-cytometric analysis was performed with mice fed a HFD for 17 weeks. (B-D) Flow-cytometric analysis of the number of total Treg cells and the fraction of ST2 + Treg cells (n=11, 10, 4, 7) (B) , the number of total CD45 + cells, the percentages of total and CD11c high macrophages (C top), the percentages of total T cells, CD8 + T cells and Foxp3 − CD4 + cells (C bottom) , and the number of total mSCs and the fraction of IL-33 + mSCs (D) One-way ANOVA was used for calculating p values ( B : **** p<0.0001, **** p<0.0001, and **** p<0.0001; C top : *** p=0.00011, *** p=0.00074, * p=0.038; **** p<0.0001, * p=0.031, and **** p<0.0001; C bottom : **** p<0.0001, * p=0.036, **** p<0.0001, **** p<0.0001, and ** p=0.0015; D : **** p<0.0001, * p<0.027, and * p<0.018). (E) GTT (top) and ITT (bottom) analyses of the indicated mice fed a HFD for 12 weeks (n=11, 10, 4, 7). Two-way ANOVA was used for calculating p values (GTT: **** p<0.0001, and ** p=0.0093; ITT: **** p<0.0001, and ** p=0.0015). Note, normalized values are presented for this plot because multiple independent cohorts were examined at diverse times. (F) RT-qPCR measuring mRNAs associated with thermogenesis and adipogenesis in iWAT of the indicated male mice received AAV-irisin or -GFP, and fed a HFD for 17 weeks (n=11, 10, 4, 7). Two-way ANOVA was used for calculating p values (p values between Il1rl1 wt AAV-GFP and Il1rl1 wt AAV-irisin, as well as Il1rl1 wt AAV-irisin and Il1rl1 Δtreg AAV-irisin: Ppargc1a : *** p=0.0004, and *** p=0.0006; Ucp1 : **** p<0.0001, and ** p=0.0043; Ckb : *** p=0.0002, and ns p=0.6285; Alpl : ** p=0.0050, and ns p=0.9976; Dio2 : ** p=0.0048, and * p=0.0123; Elovl3 : **** p<0.0001, and **** p<0.0001). Abbreviations as per Figure 1 , 2 & 3 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Unless specifically mentioned, experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Quantitative RT-PCR

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: Adipose tissues in male obese mice secrete irisin cofactor under stress, which activates irisin integrin receptor on the messenchymal stromal cells. Irisin binds and signals through the activated receptor for IL-33 production. In visceral fat tissue, the secreted soluble form of IL-33 acts on ST2 + Treg cells to protect the visceral fat Treg population and keep the visceral fat inflammation in check; in subcutaneous fat tissue, IL-33 targets the ST2 + adipocytes (and/or other ST2 + cell types) to stimulate thermogenesis and control the fat mass. None of the data exclude the possibility of the role of elevated circulating IL-33 in mediating effects in subcutaneous fat tissue.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Control

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Representative gating strategy for analyzing IL-33 + mSCs. (B) Summary data for numbers of IL-33 + mSCs in eWATs from the male mice in Extended Data Fig. 3F (n=4, 4, 8, 8). (C) Summary data for numbers of IL-33 + mSCs in iWATs and BATs from the mice in Extended Data Fig. 3F and Figure 2 (left, n=4, 4, 8, 8; right, n=3, 3, 8, 8). (D) ELISA measurements of IL-33 concentration in iWAT and BAT lysates from a subset of mice in Figure 3C (n=3, 3, 3, 3). One-way ANOVA was used for calculating p values (* p=0.0159, *** p=0.0002, and ** p=0.0050). (E) Summary data for numbers of ILC2s in eWAT, iWAT and BAT from the mice in Extended Data Fig. 4 (top, n=4, 4, 8, 8; bottom, n=3, 3, 8, 8). (F) Freshly isolated IL-33 (EGFP) − mSCs from 12 wk-old male Il33.Egfp mice were treated with PBS or 10 nM/Hsp90α irisin for 3 days, followed by flow-cytometric analysis. Left: experimental scheme; right: summary data for numbers and fractions of IL-33 (EGFP) + mSCs. n=3. Abbreviation: mSCs, mesenchymal stromal cells; ILC2s, type 2 innate lymphoid cells; other abbreviations as per Figure 1 & 2 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Unless specifically mentioned, experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Expressing, Enzyme-linked Immunosorbent Assay, Concentration Assay, Isolation

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Normalized read counts of integrin αV and β5 subunits from prior RNA-seq data 48 . One-way ANOVA was used for calculating p values (ns p=0.7013, * p=0.0234, and ** p=0.0081). (B) RT-qPCR measuring IL-33 mRNAs in flow cytometrically sorted IL-33 (EGFP) − mSCs from 12 wk-old male Il33.Egfp mice treated with PBS or 10 nM irisin/Hsp90α for 3 days in the presence of anti-αVβ5 or control IgG. One-way ANOVA was used for calculating p values (**** p<0.0001, ns p=0.9930, and **** p<0.0001). (C) Fluorescence imaging and quantification of IL-33-GFP expression of flow cytometrically isolated IL-33 (EGFP) − mSCs from 12 wk-old male Il33.Egfp mice treated with PBS or 10 nM irisin/Hsp90α for 3 days in the presence of anti-αVβ5 or control IgG. Left: representative images of the treated mSCs, Scale bar = 100 μm; Right: normalized GFP signals from each wells. One-way ANOVA was used for calculating p values (**** p<0.0001, ns p=0.9948, and *** p=0.0002). (D) Fluorescence imaging and quantification of integrin signaling of flow cytometrically isolated IL-33 (EGFP) − mSCs from 12 wk-old male Il33.Egfp mice treated with PBS or 10 nM irisin/Hsp90α for 3 days in the presence of anti-αVβ5 or control IgG. Left: representative images of the treated mSCs, Scale bar = 100 μm; Right: quantification of pFAK/FAK ratios from each wells. One-way ANOVA was used for calculating p values (**** p<0.0001, ns p=0.8338, and **** p<0.0001). Abbreviations as per Figure 1 & 2 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Unless specifically mentioned, experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Expressing, RNA Sequencing, Quantitative RT-PCR, Control, Fluorescence, Imaging, Isolation

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) Summary data of the number of total CD4 + T cells, as well as the percentages of Treg cells and ST2 + Treg cells in the spleen of the indicated mice from the flow-cytometric analysis. (B-E) 8 wk-old male Fndc5 +/+ or Fndc5 −/− littermates were treated as per Figure 4C . (B) Summary data for the number of total Treg cells and the fraction of ST2 + Treg cells in iWAT. n=3, 4, 3, 3. One-way ANOVA was used for calculating p values (* p=0.0269). (C, D) Representative gating strategy for analyzing ILC2s (C) and Eosinophils (D) . (E-F) Summary data for numbers of ST2 + Foxp3 − CD4 + cells, ILC2s, and Eosinophils in eWAT (n=9, 9, 6, 8) (E) and iWAT (n=3, 4, 3, 3) (F) . Brown-Forsythe and Welch ANOVA ( E ) or one-way ANOVA ( F ) was used for calculating p values ( E : * p=0.0238, ** p=0.0011, * p=0.0426, **** p<0.0001, and ** p=0.0011; F : * p=0.0333, * p=0.0293, and * p=0.0161). (G) ELISA measurements of irisin plasma concentrations in male Fndc5 +/+ and Fndc5 −/− mice fed a HFD for 17 weeks after AAV injection; n=10, 11, 13, 13. One-way ANOVA was used for calculating p values (*** p=0.0001, and *** p=0.0006). (H) Pearson correlation analysis of area under ITT curves and body weight of male Fndc5 −/− mice fed a HFD for 17 weeks after AAV injection; n=16. Abbreviations as per Figure 4 & 5 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Experiments in B-F were repeated three times with similar results, and the rest of the experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Enzyme-linked Immunosorbent Assay, Clinical Proteomics, Injection

Journal: Nature metabolism

Article Title: Irisin ameliorates obesity and insulin-resistance via adipose-tissue IL-33 and regulatory T cells

doi: 10.1038/s42255-026-01491-2

Figure Lengend Snippet: (A) RT-qPCR measuring mRNAs of ST2, IL-33 and genes associated with thermogenesis in different batches of differentiated primary iWAT cultures prepared from stromal vascular fraction (SVF) of 4-week-old male C57BL6 mice ; n=3, 3, 3, 3. Two-way ANOVA was used for calculating p values (left: **** p<0.0001, *** p=0.0001, and **** p<0.0001; right: ns p=0.9632, ** p=0.0019, and ** p=0.0021). (B) SVF from 4-week old male mice iWAT was differentiated in vitro with indicated Irisin/HSP90α and NE treatments (left). IL-33 mRNAs were measured using RT-qPCR (right) (n= 4, 4, 4, 4). Two-way ANOVA was used for calculating p values ( Il1rl1 : * p=0.0160, ** p=0.0016, and ** p<0.0022; Il33 : * p=0.0436, * p=0.0309, ** p=0.0042, and ** p=0.0032; Alpl : ** p=0.0080, and ** p=0.0059; Ucp1 : ** p=0.0010, ** p=0.0043, * p=0.0276, and *** p=0.0003). (C) RT-qPCR measuring ALPL mRNA in differentiated primary iWAT cultures in the presence or absence of NE treatment; n=4, 4, 4, 4. Two-way ANOVA was used for calculating p values (** p=0.0028, **** p<0.0001, and **** p<0.0001). Abbreviations: NE: norepinephrine; as well as per Figure 1 and 2 . Mean±SD.* p<0.05, ** p<0.01, *** p<0.001, **** p<0.0001, ns: not significant. Significant but irrelevant p values are not indicated. Unless specifically mentioned, experiments were repeated twice with similar results.

Article Snippet: For integrin agonist antibody treatment, 1hr prior to irisin/HSP90α or PBS treatment, the cultures were pretreatment with 1ng/ml of a control IgG (Abcam #206200) or anti-αVβ5 antibody (Abcam #177004). eWAT-Treg cells were sorted from 12wk-old Foxp3-Thy1.1 mice, cultured in RPMI1640 supplemented with 10% FBS, 50μM β-mercaptoethanol, 1% penicillin/streptomycin, 2000U/mL human recombinant IL-2 (Cat# 200-02, Peprotech)and were stimulated with anti-CD3/CD28 dynabeads (Cat# 11452D, ThermoFisher) in the presence of CM treated with either control IgG or anti-IL-33 antibody (2ug/ml, Cat# AG-27B-0013PF-C100, AdipoGen Life Sciences) from mSCs for 3 days at 37°C in a 5% CO2 atmosphere.

Techniques: Quantitative RT-PCR, In Vitro

Journal: Nature Communications

Article Title: Single-cell multiomics uncovers an endothelial mechanosensitive PIEZO1-IL-33 axis driving pulmonary fibrosis

doi: 10.1038/s41467-026-70193-w

Figure Lengend Snippet: A CellChat analysis of human lung snRNA-seq data. B Venn of 47 shared DEGs from four datasets ( GSE159354 , GSE132771 , GSE128033 , GSE122960 ). C Heatmap of 47-gene expression across cell types. D Correlation analysis (Pearson Correlation) of expression of IGFBP5, IL33, MGP, SPRY1, ACKR1 and mechanical stress scores in ECs. E Correlation analysis (Pearson Correlation) of expression of PIEZO1 and IGFBP5, IL33, MGP, SPRY1, ACKR1 in ECs. F Human snRNA-seq UMAP and violin of IL33 distribution and subpopulations. G Bar chart showed expression of IL33 (mean ± SEM) in IPF (n = 7966 cells) vs control (n = 4174 cells). P value was calculated using the two-tailed unpaired t-test. H Violin of IL33 in PIEZO1 - vs PIEZO1 + ECs. I Bulk-RNA-seq of saline and BLM (7 days and 14 days) induced mice (n = 3 per group). Gene expression levels were Z-score normalized. P value was calculated using the two-tailed unpaired t-test. J qPCR of Il33 in BLM mouse lung ECs. K IL-33 (green) and CD31 (red) co-staining in human IPF vs normal, quantification is shown at right (n = 10). L IL-33 (green) and CD31 (red) co-staining in Yoda1- or GsMTx4-treated fibrotic mouse lungs, quantification is shown at right (n = 3). M IL-33 (green) and CD31 (red)co-staining in Piezo1 WT and Piezo1 ΔEC BLM lungs, quantification is shown at right (n = 3). Error bars represent mean ± SEM, H, K, J, M: two-tailed unpaired t-test; L: one-way ANOVA followed Tukey’s multiple comparwasons test, All n values indicate biologically independent samples. Source data are provided as a Source Data file.

Article Snippet: 30–60 μg of protein was loaded per well on 4–20% SDS-PAGE gels (ACE, #ET15420LGel), transferred to ethanol-activated PVDF membranes (Thermo Fisher Scientific, #88518), blocked with 5% skim milk in TBST, and incubated overnight at 4 °C with primary antibodies diluted in TBST: IL-33 (R&D Systems, #AF3626, 1:1000), PIEZO1 (Proteintech, #15939-1-AP, 1:1 000), CALPAIN2 (Labome, #A03492, 1:1000), P-STAT3 (CST, #9134 s, 1:1000), STAT3 (Abcam, #ab68153, 1:2 000), P-STAT1 (CST, #9171, 1:1000), STAT1 (Proteintech, #10144-2-AP, 1:1000), GAPDH (Servicebio, #GB12002, 1:5000), β-actin (Proteintech, #66009-1, 1:5000), β-tubulin (CST, #2146, 1:5000).

Techniques: Gene Expression, Expressing, Control, Two Tailed Test, RNA Sequencing, Saline, Staining

Journal: Nature Communications

Article Title: Single-cell multiomics uncovers an endothelial mechanosensitive PIEZO1-IL-33 axis driving pulmonary fibrosis

doi: 10.1038/s41467-026-70193-w

Figure Lengend Snippet: A Schematic of BLM-induced fibrosis in Il33 WT vs Il33 ΔEC mice. B Il33 mRNA (n = 4) and IL-33 protein in lung ECs (n = 3). C Representative Masson/PSR images and quantification (n = 5). D αSMA immunofluorescence and quantification (n = 4). E Lung hydroxyproline content (n = 5). F Schematic: EC-specific Il33 overexpression via AAV-Tie1 in Piezo1 WT and Piezo1 ΔEC mice; 4-week pretreatment, BLM at week 4, sacrifice at week 7. G IL-33 expression in ECs, immune and epithelial cells after AAV-OE- Il33 (n = 3). H Masson/PSR images and quantification (n = 5). I αSMA immunofluorescence and quantification (n = 4). J Hydroxyproline content (n = 5). Error bars: mean ± SEM; B,G: two-tailed unpaired t-test; C,D-E,I: two-way ANOVA followed Tukey’s multiple comparisons test; H,J: three-way ANOVA followed Tukey’s multiple comparisons test. All n values indicate biologically independent samples. Source data are provided as a Source Data file.

Article Snippet: 30–60 μg of protein was loaded per well on 4–20% SDS-PAGE gels (ACE, #ET15420LGel), transferred to ethanol-activated PVDF membranes (Thermo Fisher Scientific, #88518), blocked with 5% skim milk in TBST, and incubated overnight at 4 °C with primary antibodies diluted in TBST: IL-33 (R&D Systems, #AF3626, 1:1000), PIEZO1 (Proteintech, #15939-1-AP, 1:1 000), CALPAIN2 (Labome, #A03492, 1:1000), P-STAT3 (CST, #9134 s, 1:1000), STAT3 (Abcam, #ab68153, 1:2 000), P-STAT1 (CST, #9171, 1:1000), STAT1 (Proteintech, #10144-2-AP, 1:1000), GAPDH (Servicebio, #GB12002, 1:5000), β-actin (Proteintech, #66009-1, 1:5000), β-tubulin (CST, #2146, 1:5000).

Techniques: Immunofluorescence, Over Expression, Expressing, Two Tailed Test

Journal: Nature Communications

Article Title: Single-cell multiomics uncovers an endothelial mechanosensitive PIEZO1-IL-33 axis driving pulmonary fibrosis

doi: 10.1038/s41467-026-70193-w

Figure Lengend Snippet: HUVECs under 20% stretch for 0,6,24 h or 2,12,25 kPa substrates; IL-33 secretion ( n = 3) A and mRNA (n = 3) B . C PIEZO1 knock-down with sh PIEZO1 ( n = 3). HUVECs were transduced with sh PIEZO1 for 48 h, cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch before measuring IL-33 secretion ( n = 3) D and mRNA ( n = 3) E . HUVECs were cultured on 2, 12, 25 kPa substrates for 24 h or stretched (20%) for 0, 6, 24 h, followed by measurement of calpain activity F and CAPN2 protein G ( n = 3). HUVECs (sh PIEZO1 ) were cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch, followed by measurement of calpain activity ( n = 3) H and CAPN2 protein levels ( n = 3) I . J CAPN2 knock-down with shCAPN2 ( n = 3). K HUVECs (sh CAPN2 ) were cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch, IL-33 secretion(left) and mRNA(right) ( n = 3). L Model for paracrine IL-33 regulation. M Cistrome: STAT3 predicted to drive IL-33 regulation. N intersection of top 100 motifs in BLM-treated mouse ECs with top 10 TFs. O The protein levels of P-STAT3 and STAT3 in HUVECs treated with 20% stretch for 0 and 6 hours ( n = 3). P The protein levels of P-STAT3 and STAT3 in HUVECs (sh PIEZO1 or sh CAPN2 ) treated with 20% stretch for 6 h ( n = 3). Q STAT3 knock-down with sh STAT3 ( n = 3). R HUVECs (sh STAT3 ) were cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch; IL-33 secretion(left) and mRNA(right) ( n = 3). Error bars: mean ± SEM; C , G , J , O – Q : two-tailed unpaired t-test; A , B , F : one-way ANOVA followed Šídák’s multiple comparisons test, D – E , H – I , K , R : two-way ANOVA Tukey’s multiple comparisons test. All n denote biologically independent samples. Source data are provided as a Source Data file.

Article Snippet: 30–60 μg of protein was loaded per well on 4–20% SDS-PAGE gels (ACE, #ET15420LGel), transferred to ethanol-activated PVDF membranes (Thermo Fisher Scientific, #88518), blocked with 5% skim milk in TBST, and incubated overnight at 4 °C with primary antibodies diluted in TBST: IL-33 (R&D Systems, #AF3626, 1:1000), PIEZO1 (Proteintech, #15939-1-AP, 1:1 000), CALPAIN2 (Labome, #A03492, 1:1000), P-STAT3 (CST, #9134 s, 1:1000), STAT3 (Abcam, #ab68153, 1:2 000), P-STAT1 (CST, #9171, 1:1000), STAT1 (Proteintech, #10144-2-AP, 1:1000), GAPDH (Servicebio, #GB12002, 1:5000), β-actin (Proteintech, #66009-1, 1:5000), β-tubulin (CST, #2146, 1:5000).

Techniques: Knockdown, Transduction, Cell Culture, Activity Assay, Two Tailed Test

Journal: Nature Communications

Article Title: Single-cell multiomics uncovers an endothelial mechanosensitive PIEZO1-IL-33 axis driving pulmonary fibrosis

doi: 10.1038/s41467-026-70193-w

Figure Lengend Snippet: A CellChat analysis of human lung snRNA-seq data. B Venn of 47 shared DEGs from four datasets ( GSE159354 , GSE132771 , GSE128033 , GSE122960 ). C Heatmap of 47-gene expression across cell types. D Correlation analysis (Pearson Correlation) of expression of IGFBP5, IL33, MGP, SPRY1, ACKR1 and mechanical stress scores in ECs. E Correlation analysis (Pearson Correlation) of expression of PIEZO1 and IGFBP5, IL33, MGP, SPRY1, ACKR1 in ECs. F Human snRNA-seq UMAP and violin of IL33 distribution and subpopulations. G Bar chart showed expression of IL33 (mean ± SEM) in IPF (n = 7966 cells) vs control (n = 4174 cells). P value was calculated using the two-tailed unpaired t-test. H Violin of IL33 in PIEZO1 - vs PIEZO1 + ECs. I Bulk-RNA-seq of saline and BLM (7 days and 14 days) induced mice (n = 3 per group). Gene expression levels were Z-score normalized. P value was calculated using the two-tailed unpaired t-test. J qPCR of Il33 in BLM mouse lung ECs. K IL-33 (green) and CD31 (red) co-staining in human IPF vs normal, quantification is shown at right (n = 10). L IL-33 (green) and CD31 (red) co-staining in Yoda1- or GsMTx4-treated fibrotic mouse lungs, quantification is shown at right (n = 3). M IL-33 (green) and CD31 (red)co-staining in Piezo1 WT and Piezo1 ΔEC BLM lungs, quantification is shown at right (n = 3). Error bars represent mean ± SEM, H, K, J, M: two-tailed unpaired t-test; L: one-way ANOVA followed Tukey’s multiple comparwasons test, All n values indicate biologically independent samples. Source data are provided as a Source Data file.

Article Snippet: The primary antibodies used were CD31 (Abcam, #ab9498; Servicebio, #GB13063), VE-cadherin (R&D Systems, #AF938), IL-33 (R&D Systems, #AF3626), PIEZO1(proteintech, #15939-1-AP) and αSMA (Abcam, #ab7817) antibodies.

Techniques: Gene Expression, Expressing, Control, Two Tailed Test, RNA Sequencing, Saline, Staining

Journal: Nature Communications

Article Title: Single-cell multiomics uncovers an endothelial mechanosensitive PIEZO1-IL-33 axis driving pulmonary fibrosis

doi: 10.1038/s41467-026-70193-w

Figure Lengend Snippet: A Schematic of BLM-induced fibrosis in Il33 WT vs Il33 ΔEC mice. B Il33 mRNA (n = 4) and IL-33 protein in lung ECs (n = 3). C Representative Masson/PSR images and quantification (n = 5). D αSMA immunofluorescence and quantification (n = 4). E Lung hydroxyproline content (n = 5). F Schematic: EC-specific Il33 overexpression via AAV-Tie1 in Piezo1 WT and Piezo1 ΔEC mice; 4-week pretreatment, BLM at week 4, sacrifice at week 7. G IL-33 expression in ECs, immune and epithelial cells after AAV-OE- Il33 (n = 3). H Masson/PSR images and quantification (n = 5). I αSMA immunofluorescence and quantification (n = 4). J Hydroxyproline content (n = 5). Error bars: mean ± SEM; B,G: two-tailed unpaired t-test; C,D-E,I: two-way ANOVA followed Tukey’s multiple comparisons test; H,J: three-way ANOVA followed Tukey’s multiple comparisons test. All n values indicate biologically independent samples. Source data are provided as a Source Data file.

Article Snippet: The primary antibodies used were CD31 (Abcam, #ab9498; Servicebio, #GB13063), VE-cadherin (R&D Systems, #AF938), IL-33 (R&D Systems, #AF3626), PIEZO1(proteintech, #15939-1-AP) and αSMA (Abcam, #ab7817) antibodies.

Techniques: Immunofluorescence, Over Expression, Expressing, Two Tailed Test

Journal: Nature Communications

Article Title: Single-cell multiomics uncovers an endothelial mechanosensitive PIEZO1-IL-33 axis driving pulmonary fibrosis

doi: 10.1038/s41467-026-70193-w

Figure Lengend Snippet: HUVECs under 20% stretch for 0,6,24 h or 2,12,25 kPa substrates; IL-33 secretion ( n = 3) A and mRNA (n = 3) B . C PIEZO1 knock-down with sh PIEZO1 ( n = 3). HUVECs were transduced with sh PIEZO1 for 48 h, cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch before measuring IL-33 secretion ( n = 3) D and mRNA ( n = 3) E . HUVECs were cultured on 2, 12, 25 kPa substrates for 24 h or stretched (20%) for 0, 6, 24 h, followed by measurement of calpain activity F and CAPN2 protein G ( n = 3). HUVECs (sh PIEZO1 ) were cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch, followed by measurement of calpain activity ( n = 3) H and CAPN2 protein levels ( n = 3) I . J CAPN2 knock-down with shCAPN2 ( n = 3). K HUVECs (sh CAPN2 ) were cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch, IL-33 secretion(left) and mRNA(right) ( n = 3). L Model for paracrine IL-33 regulation. M Cistrome: STAT3 predicted to drive IL-33 regulation. N intersection of top 100 motifs in BLM-treated mouse ECs with top 10 TFs. O The protein levels of P-STAT3 and STAT3 in HUVECs treated with 20% stretch for 0 and 6 hours ( n = 3). P The protein levels of P-STAT3 and STAT3 in HUVECs (sh PIEZO1 or sh CAPN2 ) treated with 20% stretch for 6 h ( n = 3). Q STAT3 knock-down with sh STAT3 ( n = 3). R HUVECs (sh STAT3 ) were cultured on 25 kPa substrates for 24 h or subjected to 6 h mechanical stretch; IL-33 secretion(left) and mRNA(right) ( n = 3). Error bars: mean ± SEM; C , G , J , O – Q : two-tailed unpaired t-test; A , B , F : one-way ANOVA followed Šídák’s multiple comparisons test, D – E , H – I , K , R : two-way ANOVA Tukey’s multiple comparisons test. All n denote biologically independent samples. Source data are provided as a Source Data file.

Article Snippet: The primary antibodies used were CD31 (Abcam, #ab9498; Servicebio, #GB13063), VE-cadherin (R&D Systems, #AF938), IL-33 (R&D Systems, #AF3626), PIEZO1(proteintech, #15939-1-AP) and αSMA (Abcam, #ab7817) antibodies.

Techniques: Knockdown, Transduction, Cell Culture, Activity Assay, Two Tailed Test